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Massive Rotator Cuff Tears clinical trials

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NCT ID: NCT05780229 Recruiting - Shoulder Disease Clinical Trials

Effectiveness of Treatments for Massive Rotator Cuff Tears: Mixed Methodology.

Start date: March 27, 2019
Phase:
Study type: Observational

The purpose of this study is: 1) to identify relevant treatment outcomes for people with massive rotator cuff tears of the shoulder joint, according to the experience of the affected people, to facilitate treatment shared decision-making during the specialist consultation in Spain; 2) to compare the effectiveness of conservative treatment, arthroscopic decompressive surgery and reverse prosthesis, in terms of patient's relevant outcomes and health-related quality of life.

NCT ID: NCT05001581 Recruiting - Clinical trials for Rotator Cuff Injuries

Irreparable Rotator Cuff Tears Treatment. Comparison of Two Methods: With and Without Biceps Tendon Augmentation

Start date: January 30, 2019
Phase: N/A
Study type: Interventional

Management of massive rotator cuff tears (MRCT) is associated with high rates of failure. The long head of the biceps tendon augmentation (LHBTA) by reinforcement of the reconstruction and additional blood supply may improve healing and provide better outcome than partial repair only.

NCT ID: NCT04571918 Recruiting - Clinical trials for Massive Rotator Cuff Tears

Arthroscopic Treatment of Massive Rotator Cuff Tears With Debridement and Biodegradable Spacer.

AMRIS
Start date: November 1, 2020
Phase: N/A
Study type: Interventional

Massive rotator cuff tears are common in the adult population. It is estimated that about 12 % of adults 60 years of age or older suffer from a rotator cuff injury. About 40 % of these injuries are classified as massive rotator cuff tears (MRCT). MRCT propose a great challenge to the affected patient and its doctor. It is a painful condition with few treatment options. The study aims to investigate the operative treatment for MRCT with the new treatment option proposed by Senecovic. Insertion of a biodegradable balloon as a subacromial spacer has proven promising results so far. To this date there is only small and non-randomized studies on the subject. AMRIS are planning to do a randomized controlled study where group A is treated with arthroscopic debridement, biceps tenotomy and biodegradable spacer, while group B, the control group are treated with arthroscopic debridement and biceps tenotomy.

NCT ID: NCT03352180 Recruiting - Clinical trials for Massive Rotator Cuff Tears

Subscapularis Tears in Large to Massive Rotator Cuff Tear

Start date: November 21, 2017
Phase: N/A
Study type: Interventional

Do concomitant subscapularis tears in large to massive rotator cuff tears affect postoperative functional and structural outcomes? Background and purpose: The subscarpularis tendon is essential force maintaining normal glenohumeral biomechanics. However, there are few studies which have addressed the outcomes of tears extending to the subscapularis tendon in massive rotator cuff tears. The purpose of this study was to assess the clinical and structural outcomes of arthroscopic reapair of massive rotator cuff tears involving the subscapulrais.